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临床试验/NCT04499183
NCT04499183Unknown不适用

A Feasibility Study on Fiber Fermentation, and Short Chain Fatty Acid Kinetics and Utilization Inside the Gut and Systemic Circulation

Wageningen University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2020年10月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
10
试验地点
1
主要终点
Relative microbiota composition and metabolites

研究概览

简要总结

Nowadays there is a strong interest in optimising human health through manipulation of non-digestible carbohydrates (NDC). NDC can be used as substrates by gut microbiota, which results in NDC degradation, production of fermentation products, such as short-chain fatty acids (SCFA), and a shift in microbiome composition and activity. It is hypothesized that SCFAs mediate parts of the beneficial effects of NDC. In mice, the influx of SCFA into the host correlated strongly with improvements of markers of the metabolic syndrome, in contrast to the concentrations of SCFA in the proximal colon. Therefore, the influx of short chain fatty acids (SCFA) into the body may be of high importance in improving metabolism. There is a need for more studies in humans to trace the life course of SCFA and their regulatory role in human metabolism. To study this inner world of bacterial products in humans, we will use a nasal-intestine catheter that can be used for delivery of components and sampling chyme in the proximal colon. Before the proposed methodology can be applied in a large intervention study, a small scale feasibility study needs to be performed that addresses colonic placement of the nasal-intestine cathether and colonic sampling of regular and NDC-enriched chyme samples. We will investigate the acute fermentation of fructo- and galacto-oligosaccharides in the proximal colon. Moreover, we will deliver 13C-labelled SCFA via a naso-intestinal catheter to quantify the fluxes of SCFA production, interconversion and uptake by the host. A small-scale, 7-day parallel feasibility trial, N=5 subjects will receive GOS/FOS supplements (mix 1:1 ratio, 15 gram/day), and N=5 other subjects will receive placebo supplements (isocaloric maltodextrin, 12 gram/day). At the last day of the supplementation period, the catheter will be placed, and afterwards participants stay maximum 5 hours in the hospital, to ensure progression of the nose-intestine catheter. After an overnight fast, subjects will visit the hospital again for measurements. Subjects will consume a NDC bolus (200 mL tap water, 5 gram fructo-oligosaccharides, 5 gram galacto-oligosaccharides, non-absorbable marker (PEG-4000). Afterwards, they are not allowed to eat for 6.5 hours. Isotopically 13C-labelled SCFAs will be delivered in the proximal colon. Blood and colonic luminal samples, breath samples, faeces and urine will be collected.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •Age 18-60yrs
  • •BMI between 18.5 and 30 kg/m2
  • •Regular bowel movement (defaecation on average once a day)
  • •Signed informed consent

排除标准

  • •Having a history of medical or surgical events that, in the opinion of the Investigator, may either put the subject at risk because of participation in the study, or influence the results of the study (e.g. diabetes, cardiovascular disease, gastrointestinal disease, renal failure, cancer, infectious disease, nose/throat).
  • •Having a history of surgical events of the gastro-intestinal tract (e.g. bariatric surgery/gastric bypass surgery)
  • •Presence of swallowing disorder
  • •Use of any prescribed or non-prescribed medication (other than paracetamol) including antacids, analgesics, and herbal remedies during the three (3) weeks prior to study start.
  • •Being lactose intolerant
  • •Follows a vegan diet
  • •Use of antibiotics within 3 months of starting the study or planned during the study
  • •Use of pro- or prebiotics (e.g. galacto-oligosaccharides, fructo-oligosaccharides)
  • •Constipation/infrequent bowel movement (less than 3 times defaecation per week)
  • •Abuse of drugs/alcohol (alcohol: >4 consumptions/day or >21 consumptions/week)
  • •Having diarrhoea within 1 month prior to the study start
  • •Personnel of Wageningen University, Division of Human Nutrition, their partner and their first and second degree relatives
  • •Participation in another biomedical study or other research from the Division of Human Nutrition
  • •Not willing to be exposed to fluoroscopy
  • •Having a hemoglobin of <8.5 mmol/L
  • •Having blood vessels that are too difficult for inserting a cannula
  • •Not having a general practitioner

研究组 & 干预措施

non-digestible carbohydrates

Experimental

fructo- and galacto-oligosaccharides

干预措施: fructo- and galacto-oligosaccharides (Dietary Supplement)

placebo

Placebo Comparator

maltodextrin

干预措施: fructo- and galacto-oligosaccharides (Dietary Supplement)

结局指标

主要结局

Relative microbiota composition and metabolites

时间窗: Between 0 and 400 minutes

Microbiota and metabolites inside the intestine

Concentrations of carbohydrates

时间窗: Between 0 and 400 minutes

mono-, di-, tri-, oligo- and polysaccharides in the intestinal lumen

Catheter placement in the colon

时间窗: After 1 week

To show placement of a naso-intestinal catheter in the proximal colon.

Concentrations of plasma metabolites

时间窗: Between 0 and 400 minutes

organic acids, amino acids, glucose, cholesterol, fatty acids and bile acids in blood

Concentrations of SCFAs

时间窗: Between 0 and 400 minutes

(13C isotopic) enrichments of SCFAs inside intestinal lumen

Volume of colon sample (mL)

时间窗: Between 0 and 400 minutes

To check whether enough material for analysis is obtained if the catheter system takes samples in the proximal colon of participants.

次要结局

  • Questionnaires about (dis)comfort of study procedures(After 1 week)
  • Concentrations of urine metabolites(After 0 and 120 minutes)
  • Relative microbiota composition and metabolite concentrations(After 1 week)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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